Low Prevalence of Celiac Disease among Patients with Functional Gastrointestinal Disorders in Latvia.


Journal

Journal of gastrointestinal and liver diseases : JGLD
ISSN: 1842-1121
Titre abrégé: J Gastrointestin Liver Dis
Pays: Romania
ID NLM: 101272825

Informations de publication

Date de publication:
13 Mar 2020
Historique:
received: 27 06 2019
accepted: 22 01 2020
entrez: 17 3 2020
pubmed: 17 3 2020
medline: 10 4 2021
Statut: epublish

Résumé

Studies suggest that the prevalence of celiac disease (CD) is increased in individuals with functional gastrointestinal disorders (FGIDs), in particular, irritable bowel syndrome (IBS); however, the evidence is conflicting. We aimed to analyze the prevalence of CD in patients with FGIDs in Latvia. This retrospective study included patients with FGIDs, referred for a gastroenterologist consultation in a secondary gastroenterology practice unit. Patients were divided into three groups - patients only with IBS (IBS group), patients only with functional dyspepsia (FD) (FD group), patients with mixed symptoms IBS and FD (Mixed group). Patient levels of tissue transglutaminase IgA (tTG-IgA) and/or antiendomysial IgA group antibodies (EMA-IgA) were evaluated. Four duodenal biopsies were obtained and reported according to Marsh classification. Patients diagnosed or being referred for confirmation of CD were excluded from the study. Overall, 1,833 FGIDs patients were enrolled. Celiac serology was available for 1,570 patients, duodenal histology for 582 patients, both histology and serology for 319 patients. In total, celiac seropositivity was present in 1.78% (28/1570) (3.18% in IBS group, 0.90% in FD group and 1.11% of cases in the mixed group). Fifteen patients had histopathological changes (2.58%; 15/582). Three IBS patients (2.36%) were both serology and biopsy positive. None of the FD patients had CD. Prevalence of biopsy-proven CD in patients from Latvia with FGIDs was low. Routine screening for CD could be considered only among patients with IBS.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Studies suggest that the prevalence of celiac disease (CD) is increased in individuals with functional gastrointestinal disorders (FGIDs), in particular, irritable bowel syndrome (IBS); however, the evidence is conflicting. We aimed to analyze the prevalence of CD in patients with FGIDs in Latvia.
METHODS METHODS
This retrospective study included patients with FGIDs, referred for a gastroenterologist consultation in a secondary gastroenterology practice unit. Patients were divided into three groups - patients only with IBS (IBS group), patients only with functional dyspepsia (FD) (FD group), patients with mixed symptoms IBS and FD (Mixed group). Patient levels of tissue transglutaminase IgA (tTG-IgA) and/or antiendomysial IgA group antibodies (EMA-IgA) were evaluated. Four duodenal biopsies were obtained and reported according to Marsh classification. Patients diagnosed or being referred for confirmation of CD were excluded from the study.
RESULTS RESULTS
Overall, 1,833 FGIDs patients were enrolled. Celiac serology was available for 1,570 patients, duodenal histology for 582 patients, both histology and serology for 319 patients. In total, celiac seropositivity was present in 1.78% (28/1570) (3.18% in IBS group, 0.90% in FD group and 1.11% of cases in the mixed group). Fifteen patients had histopathological changes (2.58%; 15/582). Three IBS patients (2.36%) were both serology and biopsy positive. None of the FD patients had CD.
CONCLUSION CONCLUSIONS
Prevalence of biopsy-proven CD in patients from Latvia with FGIDs was low. Routine screening for CD could be considered only among patients with IBS.

Identifiants

pubmed: 32176757
doi: 10.15403/jgld-233
doi:

Substances chimiques

Autoantibodies 0
Immunoglobulin A 0
Protein Glutamine gamma Glutamyltransferase 2 EC 2.3.2.13
Transglutaminases EC 2.3.2.13
GTP-Binding Proteins EC 3.6.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

33-39

Auteurs

Alise Dekante (A)

Faculty of Medicine, University of Latvia, Riga, Latvia. alise.dekante@gmail.com.

Ilva Daugule (I)

Faculty of Medicine, University of Latvia, Riga, Latvia; Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. ilva_daugule@hotmail.com.

Sergejs Pavlovics (S)

Faculty of Medicine, University of Latvia, Riga, Latvia. pavlovics.sergejs@gmail.com.

Ilze Kikuste (I)

Faculty of Medicine, University of Latvia, Riga, Latvia; Digestive Diseases Centre GASTRO, Riga, Latvia; Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. ikikuste@gmail.com.

Inese Polaka (I)

Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. inese.polaka@gmail.com.

Lilian Tzivian (L)

Faculty of Medicine, University of Latvia, Riga, Latvia; Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. liliana.civjane@lu.lv.

Ilona Kojalo (I)

Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. ilona.riga@gmail.com.

Vieturs Putnins (V)

Academical Laboratory of Histology, Riga, Latvia. putnsvst24@inbox.lv.

Ivars Tolmanis (I)

Digestive Diseases Centre GASTRO, Riga, Latvia. ivars.tolmanis@gastrocentrs.lv.

Ingrida Rumba-Rozenfelde (I)

Faculty of Medicine, University of Latvia, Riga, Latvia. ingrida.rumba-rozenfelde@lu.lv.

Sarmite Boka (S)

Faculty of Medicine, University of Latvia, Riga, Latvia. sarmitebo@gmail.com.

Aigars Vanags (A)

Digestive Diseases Centre GASTRO, Riga, Latvia; Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. mako@inbox.lv.

Marcis Leja (M)

Faculty of Medicine, University of Latvia, Riga, Latvia; Digestive Diseases Centre GASTRO, Riga, Latvia; Institute of Clinical and Preventive Medicine, University of Latvia, Riga, Latvia. cei@latnet.lv.

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Classifications MeSH